Variant report

Variant	esv3322577
Chromosome Location	chr7:99868041-99870889
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:596)
CpG islands
(count:549)
Chromatin interactive
region (count:2)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:596 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:99868232-99868445	HepG2	liver:	n/a	n/a
2	ATF3	chr7:99869654-99870002	K562	blood:	n/a	chr7:99869812-99869821
3	BACH1	chr7:99869775-99869955	H1-hESC	embryonic stem cell:	n/a	n/a
4	BCL11A	chr7:99869393-99869661	GM12878	blood:	n/a	n/a
5	BCL3	chr7:99869522-99870148	GM12878	blood:	n/a	chr7:99869953-99869966 chr7:99869950-99869963 chr7:99869957-99869970
6	BCL3	chr7:99869668-99870102	A549	lung:	n/a	chr7:99869953-99869966 chr7:99869950-99869963 chr7:99869957-99869970
7	BCLAF1	chr7:99869609-99869956	GM12878	blood:	n/a	n/a
8	BHLHE40	chr7:99869842-99870008	GM12878	blood:	n/a	chr7:99869947-99869963 chr7:99869956-99869972 chr7:99869950-99869966 chr7:99869953-99869969
9	BHLHE40	chr7:99869780-99870096	K562	blood:	n/a	chr7:99869947-99869963 chr7:99869956-99869972 chr7:99869950-99869966 chr7:99869813-99869829 chr7:99869953-99869969
10	BHLHE40	chr7:99867871-99868256	HepG2	liver:	n/a	n/a
11	CBX3	chr7:99869687-99870331	K562	blood:	n/a	n/a
12	CCNT2	chr7:99869613-99870080	K562	blood:	n/a	n/a
13	CEBPB	chr7:99869760-99869964	Hela-S3	cervix:	n/a	n/a
14	CEBPD	chr7:99869821-99870103	HepG2	liver:	n/a	n/a
15	CHD1	chr7:99869858-99870003	GM12878	blood:	n/a	n/a
16	CHD2	chr7:99869750-99870051	Hela-S3	cervix:	n/a	chr7:99869813-99869823
17	CHD2	chr7:99869757-99869958	GM12878	blood:	n/a	chr7:99869813-99869823
18	CREB1	chr7:99869593-99870103	A549	lung:	n/a	n/a
19	CTCF	chr7:99869340-99869490	HRPEpiC	eye:	n/a	chr7:99869431-99869444
20	CTCF	chr7:99869785-99870049	HepG2	liver:	n/a	n/a
21	CTCF	chr7:99869900-99870050	MCF-7	breast:	n/a	n/a
22	CTCF	chr7:99869840-99869990	HMF	breast:	n/a	n/a
23	CTCF	chr7:99869938-99870019	GM20000	blood:	n/a	n/a
24	CTCF	chr7:99869340-99869490	GM12866	blood:	n/a	chr7:99869431-99869444
25	CTCF	chr7:99869840-99869990	NHDF-neo	bronchial:	n/a	n/a
26	CTCF	chr7:99869360-99869510	NB4	blood:	n/a	chr7:99869431-99869444
27	CTCF	chr7:99869806-99870053	GM19239	blood:	n/a	n/a
28	CTCF	chr7:99869393-99869498	GM12878	blood:	n/a	chr7:99869431-99869444
29	CTCF	chr7:99869217-99870250	K562	blood:	n/a	chr7:99869431-99869444
30	CTCF	chr7:99870119-99870127	Kidney_OC	kidney:	n/a	n/a
31	CTCF	chr7:99869878-99870024	A549	lung:	n/a	n/a
32	CTCF	chr7:99869840-99869990	NB4	blood:	n/a	n/a
33	CTCF	chr7:99869822-99870060	NHEK	skin:	n/a	n/a
34	CTCF	chr7:99869880-99870030	AG04449	skin:	n/a	n/a
35	CTCF	chr7:99869884-99870027	MCF-7	breast:	n/a	n/a
36	CTCF	chr7:99869820-99869970	GM12864	blood:	n/a	n/a
37	CTCF	chr7:99869914-99870014	Gliobla	brain:	n/a	n/a
38	CTCF	chr7:99869493-99869571	LNCaP	prostate:	n/a	n/a
39	CTCF	chr7:99869860-99870010	NHLF	lung:	n/a	n/a
40	CTCF	chr7:99869901-99870004	ProgFib	skin:	n/a	n/a
41	CTCF	chr7:99869843-99870077	Pancreas_OC	pancreas:	n/a	n/a
42	CTCF	chr7:99869419-99869556	Spleen_OC	spleen:	n/a	chr7:99869431-99869444
43	CTCF	chr7:99868220-99868370	BJ	skin:	n/a	n/a
44	CTCF	chr7:99869880-99870030	K562	blood:	n/a	n/a
45	CTCF	chr7:99869340-99869490	A549	lung:	n/a	chr7:99869431-99869444
46	CTCF	chr7:99869840-99869990	GM12869	blood:	n/a	n/a
47	CTCF	chr7:99869840-99869990	GM12871	blood:	n/a	n/a
48	CTCF	chr7:99869860-99870010	GM12866	blood:	n/a	n/a
49	CTCF	chr7:99869858-99870095	GM12891	blood:	n/a	n/a
50	CTCF	chr7:99870032-99870049	GM20000	blood:	n/a	n/a

(count:549 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:99869784-99869834	SK-N-SH	brain:	n/a
2	chr7:99869529-99869579	PANC-1	pancreas:	n/a
3	chr7:99869835-99869885	BE2_C	brain:	n/a
4	chr7:99869784-99869834	PANC-1	pancreas:	n/a
5	chr7:99869784-99869834	HCF	heart:	n/a
6	chr7:99870040-99870090	T-47D	breast:	n/a
7	chr7:99870182-99870232	HCM	heart:	n/a
8	chr7:99869028-99869078	NH-A	brain:	n/a
9	chr7:99869454-99869504	SK-N-SH	brain:	n/a
10	chr7:99869835-99869885	ProgFib	skin:	n/a
11	chr7:99869454-99869504	HepG2	liver:	n/a
12	chr7:99870040-99870090	GM06990	blood:	n/a
13	chr7:99869454-99869504	T-47D	breast:	n/a
14	chr7:99870182-99870232	HNPCEpiC	eye:	n/a
15	chr7:99870057-99870107	ProgFib	skin:	n/a
16	chr7:99870147-99870197	HCPEpiC	choroid plexus:	n/a
17	chr7:99869028-99869078	HPAEpiC	pulmonary alveolar:	n/a
18	chr7:99869784-99869834	RPTEC	kidney:	n/a
19	chr7:99870040-99870090	BE2_C	brain:	n/a
20	chr7:99870147-99870197	AG10803	skin:	n/a
21	chr7:99869835-99869885	Jurkat	blood:	n/a
22	chr7:99869028-99869078	ECC-1	luminal epithelium:	n/a
23	chr7:99869529-99869579	HCF	heart:	n/a
24	chr7:99869454-99869504	HCT-116	colon:	n/a
25	chr7:99870057-99870107	T-47D	breast:	n/a
26	chr7:99870057-99870107	HCM	heart:	n/a
27	chr7:99869529-99869579	HIPEpiC	eye:	n/a
28	chr7:99869529-99869579	AG04450	lung:	fetal
29	chr7:99869784-99869834	SK-N-MC	brain:	n/a
30	chr7:99870040-99870090	Hela-S3	cervix:	n/a
31	chr7:99869835-99869885	AoSMC	blood vessel:	n/a
32	chr7:99870147-99870197	IMR90	lung:	fetal
33	chr7:99869028-99869078	ProgFib	skin:	n/a
34	chr7:99870147-99870197	RPTEC	kidney:	n/a
35	chr7:99869529-99869579	HRPEpiC	eye:	n/a
36	chr7:99869529-99869579	HEEpiC	esophagus:	n/a
37	chr7:99869028-99869078	HIPEpiC	eye:	n/a
38	chr7:99869835-99869885	RPTEC	kidney:	n/a
39	chr7:99870147-99870197	AG09319	gingival:	n/a
40	chr7:99870147-99870197	ECC-1	luminal epithelium:	n/a
41	chr7:99869454-99869504	NH-A	brain:	n/a
42	chr7:99869028-99869078	HRCEpiC	kidney:	n/a
43	chr7:99869454-99869504	AG04450	lung:	fetal
44	chr7:99870182-99870232	AG04450	lung:	fetal
45	chr7:99870182-99870232	ECC-1	luminal epithelium:	n/a
46	chr7:99869454-99869504	HRE	kidney:	n/a
47	chr7:99870182-99870232	AG09319	gingival:	n/a
48	chr7:99869454-99869504	NHDF-neo	bronchial:	n/a
49	chr7:99870182-99870232	SKMC	muscle:	n/a
50	chr7:99869784-99869834	HepG2	liver:	n/a

(count:2 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:99678858..99680502-chr7:99868393..99870017,2	K562	blood:
2	chr7:99746174..99748056-chr7:99869608..99872452,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000239521	TF binding region
GATS	TF binding region
ENSG00000239521	CpG island
GATS	CpG island
ENSG00000188186	chromatin interactions
ENSG00000166526	chromatin interactions

Extended variants
information (count: 80 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:80 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs572954373	chr7:99868096-99868097	Active TSS Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs540381320	chr7:99868147-99868148	Active TSS Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs555736644	chr7:99868238-99868239	Active TSS Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs573983621	chr7:99868252-99868253	Active TSS Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs544255889	chr7:99868336-99868337	Active TSS Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs12113906	chr7:99868412-99868413	Active TSS Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs577680606	chr7:99868427-99868428	Active TSS Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs544799335	chr7:99868446-99868447	Active TSS Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs185219311	chr7:99868535-99868536	Active TSS Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs112043149	chr7:99868556-99868557	Active TSS Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs141233430	chr7:99868574-99868575	Active TSS Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs190148579	chr7:99868575-99868576	Active TSS Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs552199161	chr7:99868681-99868682	Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs371939062	chr7:99868684-99868685	Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs182379594	chr7:99868690-99868691	Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs570502007	chr7:99868691-99868692	Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs565514191	chr7:99868695-99868696	Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs374127840	chr7:99868727-99868728	Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs112384309	chr7:99868800-99868801	Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs531868542	chr7:99868808-99868809	Active TSS Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs550025200	chr7:99868876-99868877	Active TSS Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs571328899	chr7:99868882-99868883	Active TSS Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs538975022	chr7:99868962-99868963	Active TSS Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs547582882	chr7:99869065-99869066	Active TSS Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs375646321	chr7:99869140-99869141	Active TSS Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs566152328	chr7:99869190-99869191	Active TSS Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs13234011	chr7:99869192-99869193	Active TSS Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs533791128	chr7:99869252-99869253	Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs13234110	chr7:99869259-99869260	Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs4084978	chr7:99869268-99869269	Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs555581711	chr7:99869269-99869270	Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs574020730	chr7:99869289-99869290	Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs13234340	chr7:99869375-99869376	Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs538157829	chr7:99869389-99869390	Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs200171016	chr7:99869446-99869447	Active TSS Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs3735244	chr7:99869455-99869456	Active TSS Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs368589202	chr7:99869456-99869457	Active TSS Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs372345895	chr7:99869465-99869466	Active TSS Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs544948862	chr7:99869502-99869503	Active TSS Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs376366977	chr7:99869513-99869514	Active TSS Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs368369600	chr7:99869520-99869521	Active TSS Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs371961029	chr7:99869551-99869552	Active TSS Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs376811492	chr7:99869568-99869569	Active TSS Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs199808373	chr7:99869589-99869590	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs572105615	chr7:99869590-99869591	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs369388870	chr7:99869595-99869596	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs373123333	chr7:99869597-99869598	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs542885823	chr7:99869600-99869601	Active TSS Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs376626284	chr7:99869609-99869610	Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs35408185	chr7:99869655-99869656	Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:95)

Disease	PMID	Source
Basal cell lymphoma	17170743	CNVD
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
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Non-small cell lung cancer	21829676	CNVD
Gastric cancer	24379144	CNVD
Glioblastoma multiforme	17002787	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	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
small cell lung cancer	20016488	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
Metanephric adenoma	20802469	CNVD
Prostate cancer	16461572	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Malignant melanoma	17260012	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Chronic myeloid leukemia	21384125	CNVD
Bladder cancer	21909424	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Biliary cancer	19435499	CNVD
Myelofibrosis	22110671	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	16608533	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Liver carcinoma	19366792	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Adenocarcinoma	19607727	CNVD
Multiple myeloma	16461302	CNVD
Breast cancer	21858162	CNVD
Emphysema	19352772	CNVD
Effusion lymphoma	18079361	CNVD
Medulloblastoma	17653508	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Autism	19401682	CNVD
Neuroticism	17667963	CNVD
Breast cancer	21509527	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Prostate cancer	18632612	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Melanoma	20877625	CNVD

Chromatin state (count:482 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:99833000-99868600	Weak transcription	Primary T cells from cord blood	blood
2	chr7:99833200-99868600	Weak transcription	Thymus	Thymus
3	chr7:99842000-99868400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
4	chr7:99845200-99868200	Weak transcription	Primary neutrophils fromperipheralblood	blood
5	chr7:99845400-99868200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr7:99846400-99868800	Weak transcription	Right Ventricle	heart
7	chr7:99847000-99868200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr7:99851800-99868400	Weak transcription	Primary T helper cells fromperipheralblood	blood
9	chr7:99852600-99868400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
10	chr7:99853400-99868400	Weak transcription	Primary B cells from cord blood	blood
11	chr7:99858200-99868200	Weak transcription	H9 Cell Line	embryonic stem cell
12	chr7:99858400-99868400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
13	chr7:99858600-99868200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr7:99859000-99868400	Weak transcription	Esophagus	oesophagus
15	chr7:99861400-99868400	Enhancers	Placenta	Placenta
16	chr7:99862800-99869200	Weak transcription	Lung	lung
17	chr7:99863000-99868400	Weak transcription	NHEK	skin
18	chr7:99864000-99868200	Enhancers	Pancreas	Pancrea
19	chr7:99864600-99868200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
20	chr7:99864600-99868200	Weak transcription	Right Atrium	heart
21	chr7:99864600-99868200	Weak transcription	NHLF	lung
22	chr7:99864600-99868400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
23	chr7:99864600-99868600	Weak transcription	Primary B cells from peripheral blood	blood
24	chr7:99865000-99869400	Weak transcription	Spleen	Spleen
25	chr7:99866800-99868200	Enhancers	Fetal Brain Male	brain
26	chr7:99866800-99868400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr7:99866800-99868600	Enhancers	Fetal Stomach	stomach
28	chr7:99866800-99870600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr7:99867000-99868200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr7:99867000-99868800	Flanking Active TSS	Hela-S3	cervix
31	chr7:99867200-99868200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
32	chr7:99867200-99868200	Enhancers	Fetal Muscle Leg	muscle
33	chr7:99867200-99868200	Enhancers	NH-A	brain
34	chr7:99867200-99868400	Enhancers	Fetal Muscle Trunk	muscle
35	chr7:99867200-99868800	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr7:99867200-99869000	Enhancers	Stomach Mucosa	stomach
37	chr7:99867400-99868200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr7:99867400-99868200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr7:99867400-99868200	Weak transcription	Duodenum Smooth Muscle	Duodenum
40	chr7:99867400-99868400	Enhancers	HMEC	breast
41	chr7:99867400-99868600	Enhancers	Rectal Mucosa Donor 31	rectum
42	chr7:99867400-99868600	Enhancers	K562	blood
43	chr7:99867400-99868800	Enhancers	Fetal Lung	lung
44	chr7:99867400-99870000	Active TSS	Brain Germinal Matrix	brain
45	chr7:99867400-99870200	Active TSS	Rectal Smooth Muscle	rectum
46	chr7:99867400-99870200	Active TSS	HepG2	liver
47	chr7:99867600-99868200	Weak transcription	H1 Cell Line	embryonic stem cell
48	chr7:99867600-99868200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
49	chr7:99867600-99868200	Enhancers	iPS-20b Cell Line	embryonic stem cell
50	chr7:99867600-99868200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell

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