Variant report

Variant	nsv831152
Chromosome Location	chr7:137884311-138033117
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1620)
CpG islands
(count:183)
Chromatin interactive
region (count:45)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1620 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:137930021-137931102	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:137910862-137911104	K562	blood:	n/a	n/a
3	ARID3A	chr7:137930558-137930586	K562	blood:	n/a	n/a
4	ARID3A	chr7:137928134-137928510	HepG2	liver:	n/a	n/a
5	ARID3A	chr7:137920714-137921045	HepG2	liver:	n/a	n/a
6	ARID3A	chr7:137942111-137943150	K562	blood:	n/a	n/a
7	ARID3A	chr7:138013061-138013405	HepG2	liver:	n/a	n/a
8	ARID3A	chr7:138000832-138002097	HepG2	liver:	n/a	chr7:138001986-138002002
9	ARID3A	chr7:137979278-137979630	HepG2	liver:	n/a	n/a
10	ARID3A	chr7:137922760-137923024	HepG2	liver:	n/a	n/a
11	ARID3A	chr7:137998866-137999439	K562	blood:	n/a	n/a
12	ARID3A	chr7:137923950-137924143	K562	blood:	n/a	n/a
13	ARID3A	chr7:137942067-137942879	HepG2	liver:	n/a	n/a
14	ARID3A	chr7:137928072-137928595	K562	blood:	n/a	n/a
15	ARID3A	chr7:137963629-137963637	K562	blood:	n/a	n/a
16	ARID3A	chr7:137982261-137982550	HepG2	liver:	n/a	n/a
17	ATF1	chr7:137934839-137935013	K562	blood:	n/a	n/a
18	ATF1	chr7:137932817-137932950	K562	blood:	n/a	n/a
19	ATF1	chr7:137942185-137943098	K562	blood:	n/a	n/a
20	ATF1	chr7:137928201-137928662	K562	blood:	n/a	n/a
21	ATF1	chr7:137939320-137939457	K562	blood:	n/a	n/a
22	ATF1	chr7:137910783-137911126	K562	blood:	n/a	n/a
23	ATF1	chr7:137970315-137970429	K562	blood:	n/a	n/a
24	ATF1	chr7:137998883-137999397	K562	blood:	n/a	n/a
25	ATF2	chr7:137892072-137892758	H1-hESC	embryonic stem cell:	n/a	n/a
26	ATF2	chr7:137890340-137890881	H1-hESC	embryonic stem cell:	n/a	n/a
27	ATF2	chr7:137927981-137928768	H1-hESC	embryonic stem cell:	n/a	n/a
28	ATF2	chr7:137892018-137893514	H1-hESC	embryonic stem cell:	n/a	n/a
29	ATF2	chr7:137928067-137928800	H1-hESC	embryonic stem cell:	n/a	n/a
30	ATF2	chr7:137892806-137893480	H1-hESC	embryonic stem cell:	n/a	n/a
31	ATF3	chr7:137928176-137928571	K562	blood:	n/a	n/a
32	ATF3	chr7:137942171-137942868	K562	blood:	n/a	n/a
33	BACH1	chr7:137917124-137917300	K562	blood:	n/a	n/a
34	BACH1	chr7:137923990-137924258	H1-hESC	embryonic stem cell:	n/a	n/a
35	BACH1	chr7:137998973-137999022	K562	blood:	n/a	n/a
36	BACH1	chr7:137932057-137932161	K562	blood:	n/a	n/a
37	BATF	chr7:137943568-137943811	GM12878	blood:	n/a	n/a
38	BCL11A	chr7:137928197-137928576	H1-hESC	embryonic stem cell:	n/a	n/a
39	BCL11A	chr7:137892211-137892581	H1-hESC	embryonic stem cell:	n/a	n/a
40	BCL11A	chr7:137892134-137892520	H1-hESC	embryonic stem cell:	n/a	n/a
41	BCL11A	chr7:137890436-137890614	H1-hESC	embryonic stem cell:	n/a	n/a
42	BCL11A	chr7:137890396-137890768	H1-hESC	embryonic stem cell:	n/a	n/a
43	BCL11A	chr7:137893126-137893343	H1-hESC	embryonic stem cell:	n/a	n/a
44	BCL11A	chr7:137892983-137893367	H1-hESC	embryonic stem cell:	n/a	n/a
45	BCL3	chr7:137942275-137942837	K562	blood:	n/a	n/a
46	BCL3	chr7:137942323-137942733	K562	blood:	n/a	n/a
47	BCLAF1	chr7:137942038-137942837	K562	blood:	n/a	n/a
48	BHLHE40	chr7:137942196-137942754	HepG2	liver:	n/a	n/a
49	BHLHE40	chr7:137910753-137911045	K562	blood:	n/a	n/a
50	BHLHE40	chr7:137930487-137930806	HepG2	liver:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:137984018-137984068	MCF10A-Er-Src	breast:	n/a
2	chr7:137983235-137983285	SK-N-SH	brain:	n/a
3	chr7:137984018-137984068	HepG2	liver:	n/a
4	chr7:137984018-137984068	A549	lung:	n/a
5	chr7:137931748-137931798	U87	brain:	n/a
6	chr7:137983235-137983285	HIPEpiC	eye:	n/a
7	chr7:137983235-137983285	ProgFib	skin:	n/a
8	chr7:137984018-137984068	GM19239	blood:	n/a
9	chr7:137983235-137983285	ECC-1	luminal epithelium:	n/a
10	chr7:137931748-137931798	HRE	kidney:	n/a
11	chr7:137931748-137931798	HCT-116	colon:	n/a
12	chr7:137984018-137984068	GM12891	blood:	n/a
13	chr7:137984018-137984068	HCT-116	colon:	n/a
14	chr7:137931748-137931798	SKMC	muscle:	n/a
15	chr7:137983235-137983285	PrEC	prostate:	n/a
16	chr7:137983235-137983285	HMEC	breast:	n/a
17	chr7:137931748-137931798	HMEC	breast:	n/a
18	chr7:137931748-137931798	SAEC	small airway:	n/a
19	chr7:137931748-137931798	HCM	heart:	n/a
20	chr7:137984018-137984068	HRE	kidney:	n/a
21	chr7:137983235-137983285	AG04450	lung:	fetal
22	chr7:137983235-137983285	Jurkat	blood:	n/a
23	chr7:137931748-137931798	AG04449	skin:	fetal
24	chr7:137931748-137931798	IMR90	lung:	fetal
25	chr7:137931748-137931798	HEEpiC	esophagus:	n/a
26	chr7:137984018-137984068	GM06990	blood:	n/a
27	chr7:137931748-137931798	HRPEpiC	eye:	n/a
28	chr7:137983235-137983285	HL-60	blood:	n/a
29	chr7:137984018-137984068	AoSMC	blood vessel:	n/a
30	chr7:137984018-137984068	HRCEpiC	kidney:	n/a
31	chr7:137984018-137984068	U87	brain:	n/a
32	chr7:137931748-137931798	HPAEpiC	pulmonary alveolar:	n/a
33	chr7:137984018-137984068	AG09319	gingival:	n/a
34	chr7:137983235-137983285	HUVEC	blood vessel:	n/a
35	chr7:137983235-137983285	AG09309	skin:	n/a
36	chr7:137931748-137931798	H1-hESC	embryonic stem cell:	embryo
37	chr7:137983235-137983285	AoSMC	blood vessel:	n/a
38	chr7:137931748-137931798	GM19239	blood:	n/a
39	chr7:137984018-137984068	Hepatocyte	liver:	n/a
40	chr7:137983235-137983285	NHBE	bronchial:	n/a
41	chr7:137983235-137983285	BJ	skin:	n/a
42	chr7:137984018-137984068	AG04449	skin:	fetal
43	chr7:137931748-137931798	CMK	blood:	n/a
44	chr7:137983235-137983285	SK-N-MC	brain:	n/a
45	chr7:137984018-137984068	MCF-7	breast:	n/a
46	chr7:137983235-137983285	HepG2	liver:	n/a
47	chr7:137984018-137984068	NT2-D1	testis:	n/a
48	chr7:137931748-137931798	T-47D	breast:	n/a
49	chr7:137984018-137984068	ECC-1	luminal epithelium:	n/a
50	chr7:137931748-137931798	MCF10A-Er-Src	breast:	n/a

(count:45 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:137882044..137884958-chr7:138144959..138146876,2	MCF-7	breast:
2	chr7:137919927..137921486-chr7:137928600..137931150,2	MCF-7	breast:
3	chr7:137965863..137967594-chr7:137968478..137970711,2	MCF-7	breast:
4	chr7:137926916..137928434-chr7:137998152..138000341,2	K562	blood:
5	chr7:138033084..138034621-chr7:138145195..138147214,2	K562	blood:
6	chr7:137947555..137949067-chr7:137952751..137956382,3	K562	blood:
7	chr7:137995053..137999099-chr7:138144129..138146392,3	K562	blood:
8	chr7:137970347..137972756-chr7:137980665..137982972,2	K562	blood:
9	chr7:138030718..138033704-chr7:138034861..138038720,3	K562	blood:
10	chr7:137919927..137921486-chr7:137928600..137931150,2	MCF-7	breast:
11	chr7:137920098..137922481-chr7:137970184..137972526,2	MCF-7	breast:
12	chr7:137927382..137930242-chr7:137937479..137939560,2	MCF-7	breast:
13	chr7:137988083..137990941-chr7:138145037..138146557,2	MCF-7	breast:
14	chr7:137878463..137879263-chr7:137929966..137930618,2	MCF-7	breast:
15	chr7:137917155..137919916-chr7:137928733..137931455,2	MCF-7	breast:
16	chr7:137928244..137930040-chr7:137931548..137933077,2	K562	blood:
17	chr7:137978354..137980372-chr7:137985691..137988661,2	K562	blood:
18	chr7:137929429..137931956-chr7:138145009..138148414,3	MCF-7	breast:
19	chr7:137970347..137972756-chr7:137980665..137982972,2	K562	blood:
20	chr7:137942710..137944312-chr7:138144194..138147035,2	K562	blood:
21	chr7:137947637..137950178-chr7:138143942..138146389,2	K562	blood:
22	chr7:137978354..137980840-chr7:137985937..137988661,2	K562	blood:
23	chr7:137956498..137958305-chr7:137960190..137962007,2	K562	blood:
24	chr7:137891304..137893793-chr7:138144559..138146749,2	MCF-7	breast:
25	chr7:137947555..137949067-chr7:137952751..137956382,3	K562	blood:
26	chr7:137978354..137980840-chr7:137985937..137988661,2	K562	blood:
27	chr7:137854218..137856013-chr7:137925326..137928137,2	MCF-7	breast:
28	chr7:137898688..137901655-chr7:137914891..137916858,2	MCF-7	breast:
29	chr7:137974611..137977011-chr7:138155722..138157358,2	K562	blood:
30	chr7:137927382..137930242-chr7:137937479..137939560,2	MCF-7	breast:
31	chr7:137956498..137958305-chr7:137960190..137962007,2	K562	blood:
32	chr7:137912559..137915122-chr7:138143152..138145468,2	MCF-7	breast:
33	chr7:137943142..137945844-chr7:137949610..137951608,2	K562	blood:
34	chr7:137969521..137971635-chr7:138143799..138146467,2	K562	blood:
35	chr7:137943142..137945844-chr7:137949610..137951608,2	K562	blood:
36	chr7:137917155..137919916-chr7:137928733..137931455,2	MCF-7	breast:
37	chr7:137926916..137928434-chr7:137998152..138000341,2	K562	blood:
38	chr7:137898688..137901655-chr7:137914891..137916858,2	MCF-7	breast:
39	chr7:137878389..137879265-chr7:137929966..137930816,6	MCF-7	breast:
40	chr7:137928244..137930040-chr7:137931548..137933077,2	K562	blood:
41	chr7:137941053..137942559-chr7:138036086..138038896,2	K562	blood:
42	chr7:137920098..137922481-chr7:137970184..137972526,2	MCF-7	breast:
43	chr7:137965863..137967594-chr7:137968478..137970711,2	MCF-7	breast:
44	chr7:137978354..137980372-chr7:137985691..137988661,2	K562	blood:
45	chr7:138011680..138013976-chr7:138143884..138146522,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000213238	TF binding region
ENSG00000213238	CpG island
ENSG00000122779	chromatin interactions

Extended variants
information (count: 6347 )
Associated
traits (count: 99 )

Variant overlapped rSNPs/rCNVs (count:6347 , 50 per page) page: 1 2 3 4 5 6 7 ... 127

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs542454968	chr7:137884320-137884321	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs376933293	chr7:137884386-137884387	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs72315152	chr7:137884412-137884413	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs61059775	chr7:137884419-137884420	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs36065477	chr7:137884423-137884424	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs369325672	chr7:137884425-137884426	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs141106810	chr7:137884427-137884428	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs201915653	chr7:137884428-137884429	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs368375085	chr7:137884429-137884430	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs57661975	chr7:137884439-137884440	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs367760533	chr7:137884449-137884450	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs185635977	chr7:137884504-137884505	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs575953468	chr7:137884516-137884517	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs544939865	chr7:137884536-137884537	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs565170446	chr7:137884617-137884618	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs140561290	chr7:137884690-137884691	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs527314947	chr7:137884733-137884734	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs554229526	chr7:137884768-137884769	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs113640981	chr7:137884783-137884784	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs561003667	chr7:137884792-137884793	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs145633566	chr7:137884804-137884805	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs549604826	chr7:137884822-137884823	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs569449485	chr7:137884860-137884861	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs570538877	chr7:137884864-137884865	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs190101914	chr7:137884894-137884895	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs536490594	chr7:137884963-137884964	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs138119581	chr7:137884966-137884967	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs533985755	chr7:137884979-137884980	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs2352475	chr7:137884981-137884982	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs556101424	chr7:137884995-137884996	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs149537133	chr7:137885007-137885008	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs73452738	chr7:137885037-137885038	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs182360740	chr7:137885040-137885041	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs185887816	chr7:137885089-137885090	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs566959699	chr7:137885112-137885113	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs1906890	chr7:137885142-137885143	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs545166224	chr7:137885146-137885147	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs117080478	chr7:137885179-137885180	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs1906889	chr7:137885181-137885182	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs572409130	chr7:137885224-137885225	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs560816956	chr7:137885233-137885234	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs529838705	chr7:137885256-137885257	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs192108707	chr7:137885267-137885268	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs143170513	chr7:137885291-137885292	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs531841578	chr7:137885313-137885314	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs556292931	chr7:137885345-137885346	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs148250111	chr7:137885400-137885401	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs142795584	chr7:137885452-137885453	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs77558001	chr7:137885494-137885495	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs547391337	chr7:137885504-137885505	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:99)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Melanoma	19188590	CNVD
Glioblastoma multiforme	18628472	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Malignant melanoma	17260012	CNVD
Coffin-Siris syndrome	21572526	CNVD
Papillary thyroid carcinoma	21436994	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Hodgkin''s lymphoma	18179710	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	16272173	CNVD
Myxofibrosarcoma	16751306	CNVD
Stuttering	21108403	CNVD
Breast cancer	17603634	CNVD
Urothelial carcinoma	18382360	CNVD
Neuroticism	17667963	CNVD
Myelodysplastic syndrome	17634407	CNVD
Acute myeloid leukemia	17237825	CNVD
Esophageal cancer	21851588	CNVD
Bladder cancer	21909424	CNVD
Cancer	21129771	CNVD
Myelofibrosis	22110671	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
T-cell acute lymphoblastic leukemia	16673021	CNVD
Cancer	21183584	CNVD
Intracranial ependymoma	16609018	CNVD
Non-small cell lung cancer	21829676	CNVD
Developmental delay	19490664	CNVD
Pancreatitis	20877625	CNVD
Multiple myeloma	16461302	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Acute promyelocytic leukemia	20824076	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:731 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:137873600-137893800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr7:137880400-137888600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
3	chr7:137880400-137893800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr7:137882200-137887800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr7:137882800-137887600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr7:137883600-137887400	Weak transcription	Monocytes-CD14+_RO01746	blood
7	chr7:137884000-137887400	Weak transcription	Primary monocytes fromperipheralblood	blood
8	chr7:137886200-137886400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr7:137886400-137886600	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
10	chr7:137886400-137886600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr7:137886600-137887600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr7:137886600-137888000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
13	chr7:137887400-137887600	Enhancers	Monocytes-CD14+_RO01746	blood
14	chr7:137887400-137888600	Enhancers	Primary monocytes fromperipheralblood	blood
15	chr7:137887600-137888400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
16	chr7:137887600-137888600	Enhancers	H1 Cell Line	embryonic stem cell
17	chr7:137887600-137888600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
18	chr7:137887600-137889600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
19	chr7:137887600-137891000	Enhancers	iPS-15b Cell Line	embryonic stem cell
20	chr7:137887800-137888400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr7:137888000-137890600	Enhancers	HUES64 Cell Line	embryonic stem cell
22	chr7:137888000-137891000	Enhancers	ES-I3 Cell Line	embryonic stem cell
23	chr7:137888000-137891200	Enhancers	HUES6 Cell Line	embryonic stem cell
24	chr7:137888200-137888600	Enhancers	H9 Cell Line	embryonic stem cell
25	chr7:137888200-137891000	Enhancers	HUES48 Cell Line	embryonic stem cell
26	chr7:137888400-137888600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr7:137888400-137888600	Enhancers	Monocytes-CD14+_RO01746	blood
28	chr7:137888600-137889600	Weak transcription	H1 Cell Line	embryonic stem cell
29	chr7:137888600-137890000	Enhancers	iPS-20b Cell Line	embryonic stem cell
30	chr7:137888600-137890200	Enhancers	iPS-18 Cell Line	embryonic stem cell
31	chr7:137888600-137890200	Weak transcription	Primary monocytes fromperipheralblood	blood
32	chr7:137888600-137890400	Weak transcription	Monocytes-CD14+_RO01746	blood
33	chr7:137888600-137892600	Weak transcription	H9 Cell Line	embryonic stem cell
34	chr7:137888600-137893200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
35	chr7:137889000-137889200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
36	chr7:137889000-137890800	Enhancers	Cortex derived primary cultured neurospheres	brain
37	chr7:137889200-137890200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
38	chr7:137889200-137891000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr7:137889400-137889600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr7:137889400-137889600	Enhancers	NH-A	brain
41	chr7:137889400-137890800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr7:137889600-137890200	Weak transcription	NH-A	brain
43	chr7:137889600-137890600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
44	chr7:137889600-137891000	Enhancers	H1 Cell Line	embryonic stem cell
45	chr7:137889600-137891000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
46	chr7:137889600-137892000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr7:137889800-137890000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
48	chr7:137890000-137890400	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
49	chr7:137890200-137890800	Enhancers	NH-A	brain
50	chr7:137890200-137891000	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell

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