Variant report

Variant	nsv1012865
Chromosome Location	chr4:9429299-9794181
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2897)
CpG islands
(count:7084)
Chromatin interactive
region (count:40)
LncRNA
region (count:11)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:2897 , 50 per page) page: 1 2 3 4 5 6 7 ... 58

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:9454189-9454353	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:9705188-9705304	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:9764889-9764976	K562	blood:	n/a	n/a
4	ATF1	chr4:9758253-9758343	K562	blood:	n/a	n/a
5	ATF1	chr4:9693437-9693703	K562	blood:	n/a	n/a
6	ATF2	chr4:9764713-9765001	GM12878	blood:	n/a	n/a
7	BACH1	chr4:9605857-9606056	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr4:9533750-9534097	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr4:9689846-9689882	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr4:9784048-9784153	H1-hESC	embryonic stem cell:	n/a	n/a
11	BATF	chr4:9606281-9606749	GM12878	blood:	n/a	n/a
12	BATF	chr4:9496997-9497347	GM12878	blood:	n/a	n/a
13	BATF	chr4:9606359-9606745	GM12878	blood:	n/a	n/a
14	BATF	chr4:9547853-9548038	GM12878	blood:	n/a	n/a
15	BATF	chr4:9560693-9560899	GM12878	blood:	n/a	n/a
16	BATF	chr4:9582796-9583040	GM12878	blood:	n/a	n/a
17	BATF	chr4:9582818-9583030	GM12878	blood:	n/a	n/a
18	BATF	chr4:9609959-9610276	GM12878	blood:	n/a	n/a
19	BATF	chr4:9609924-9610228	GM12878	blood:	n/a	n/a
20	BATF	chr4:9709608-9710002	GM12878	blood:	n/a	n/a
21	BATF	chr4:9560631-9560870	GM12878	blood:	n/a	n/a
22	BATF	chr4:9511928-9512224	GM12878	blood:	n/a	n/a
23	BATF	chr4:9779146-9779367	GM12878	blood:	n/a	n/a
24	BATF	chr4:9661377-9661663	GM12878	blood:	n/a	n/a
25	BATF	chr4:9709684-9709950	GM12878	blood:	n/a	n/a
26	BATF	chr4:9637521-9637725	GM12878	blood:	n/a	n/a
27	BATF	chr4:9605704-9606128	GM12878	blood:	n/a	n/a
28	BATF	chr4:9431784-9432036	GM12878	blood:	n/a	n/a
29	BATF	chr4:9481132-9481453	GM12878	blood:	n/a	n/a
30	BATF	chr4:9697635-9697868	GM12878	blood:	n/a	n/a
31	BATF	chr4:9481131-9481403	GM12878	blood:	n/a	n/a
32	BATF	chr4:9715614-9715953	GM12878	blood:	n/a	n/a
33	BATF	chr4:9456872-9457051	GM12878	blood:	n/a	n/a
34	BATF	chr4:9661312-9661676	GM12878	blood:	n/a	n/a
35	BATF	chr4:9511904-9512243	GM12878	blood:	n/a	n/a
36	BCL11A	chr4:9497025-9497432	GM12878	blood:	n/a	chr4:9497121-9497129
37	BCL11A	chr4:9693955-9694191	GM12878	blood:	n/a	n/a
38	BCL11A	chr4:9709736-9710003	GM12878	blood:	n/a	n/a
39	BCL11A	chr4:9609991-9610319	GM12878	blood:	n/a	n/a
40	BCL11A	chr4:9547498-9547747	GM12878	blood:	n/a	n/a
41	BCL11A	chr4:9609970-9610277	GM12878	blood:	n/a	n/a
42	BCL11A	chr4:9637557-9637806	GM12878	blood:	n/a	n/a
43	BCL11A	chr4:9661303-9661712	GM12878	blood:	n/a	n/a
44	BCL11A	chr4:9709714-9709970	GM12878	blood:	n/a	n/a
45	BCL11A	chr4:9779122-9779297	GM12878	blood:	n/a	n/a
46	BCL11A	chr4:9606478-9606683	GM12878	blood:	n/a	n/a
47	BCL11A	chr4:9605779-9606088	GM12878	blood:	n/a	n/a
48	BCL11A	chr4:9605814-9606174	GM12878	blood:	n/a	n/a
49	BCL11A	chr4:9606348-9606693	GM12878	blood:	n/a	n/a
50	BCL3	chr4:9747374-9747670	GM12878	blood:	n/a	n/a

(count:7084 , 50 per page) page: 1 2 3 4 5 6 7 ... 142

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:9509896-9509946	NB4	blood:	n/a
2	chr4:9602138-9602188	PFSK-1	brain:	n/a
3	chr4:9653008-9653058	HEK293	kidney:	embryo
4	chr4:9707741-9707791	ovcar-3	ovarian:	n/a
5	chr4:9508976-9509026	GM19239	blood:	n/a
6	chr4:9484955-9485005	NH-A	brain:	n/a
7	chr4:9485487-9485537	Jurkat	blood:	n/a
8	chr4:9495205-9495255	SK-N-MC	brain:	n/a
9	chr4:9509896-9509946	NB4	blood:	n/a
10	chr4:9602138-9602188	PFSK-1	brain:	n/a
11	chr4:9653008-9653058	HEK293	kidney:	embryo
12	chr4:9707741-9707791	ovcar-3	ovarian:	n/a
13	chr4:9508976-9509026	GM19239	blood:	n/a
14	chr4:9484955-9485005	NH-A	brain:	n/a
15	chr4:9485487-9485537	Jurkat	blood:	n/a
16	chr4:9495205-9495255	SK-N-MC	brain:	n/a
17	chr4:9510844-9510894	HPAEpiC	pulmonary alveolar:	n/a
18	chr4:9787734-9787784	HMEC	breast:	n/a
19	chr4:9510286-9510336	SKMC	muscle:	n/a
20	chr4:9602138-9602188	SK-N-SH	brain:	n/a
21	chr4:9494211-9494261	GM19239	blood:	n/a
22	chr4:9787734-9787784	HAEpiC	amniotic membrane:	n/a
23	chr4:9558893-9558943	GM12892	blood:	n/a
24	chr4:9481822-9481872	CMK	blood:	n/a
25	chr4:9475346-9475396	IMR90	lung:	fetal
26	chr4:9508240-9508290	HUVEC	blood vessel:	n/a
27	chr4:9499194-9499244	AG04450	lung:	fetal
28	chr4:9497357-9497407	SK-N-MC	brain:	n/a
29	chr4:9485487-9485537	NB4	blood:	n/a
30	chr4:9510572-9510622	HCF	heart:	n/a
31	chr4:9760019-9760069	Hela-S3	cervix:	n/a
32	chr4:9457681-9457731	RPTEC	kidney:	n/a
33	chr4:9557805-9557855	NH-A	brain:	n/a
34	chr4:9509787-9509837	HAEpiC	amniotic membrane:	n/a
35	chr4:9479622-9479672	AG10803	skin:	n/a
36	chr4:9653008-9653058	HIPEpiC	eye:	n/a
37	chr4:9534313-9534363	SK-N-SH	brain:	n/a
38	chr4:9783363-9783413	HepG2	liver:	n/a
39	chr4:9787734-9787784	T-47D	breast:	n/a
40	chr4:9604432-9604482	RPTEC	kidney:	n/a
41	chr4:9693516-9693566	SK-N-MC	brain:	n/a
42	chr4:9509830-9509880	HNPCEpiC	eye:	n/a
43	chr4:9508240-9508290	MCF-7	breast:	n/a
44	chr4:9534651-9534701	MCF-7	breast:	n/a
45	chr4:9453084-9453134	HepG2	liver:	n/a
46	chr4:9534388-9534438	LNCaP	prostate:	n/a
47	chr4:9508177-9508227	HEEpiC	esophagus:	n/a
48	chr4:9782891-9782941	AG04450	lung:	fetal
49	chr4:9534062-9534112	NB4	blood:	n/a
50	chr4:9500465-9500515	ovcar-3	ovarian:	n/a

(count:40 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:91817635..91819182-chr4:9766044..9767255,9	MCF-7	breast:
2	chr4:9765483..9767943-chr4:10007316..10009788,2	MCF-7	breast:
3	chr2:91815622..91818416-chr4:9765055..9766802,2	K562	blood:
4	chr4:9705037..9705657-chr4:9778184..9778690,2	K562	blood:
5	chr4:9763456..9766236-chr4:10014004..10016919,3	K562	blood:
6	chr2:91816443..91817305-chr4:9764390..9765414,6	MCF-7	breast:
7	chr4:9764793..9765717-chr4:10015113..10016017,3	MCF-7	breast:
8	chr4:9699934..9701585-chr4:10019007..10021805,2	K562	blood:
9	chr4:9704779..9705714-chr4:10015117..10016069,5	MCF-7	breast:
10	chr4:9764417..9765133-chr4:10016121..10017439,5	MCF-7	breast:
11	chr2:91816088..91820118-chr4:9765029..9767622,10	MCF-7	breast:
12	chr4:4147498..4148004-chr4:9497288..9497793,2	MCF-7	breast:
13	chr4:9770192..9773137-chr4:10024212..10026749,2	K562	blood:
14	chr4:9766485..9767197-chr4:10016698..10017481,2	MCF-7	breast:
15	chr4:9764445..9765327-chr4:10020033..10020988,3	K562	blood:
16	chr4:4147469..4148009-chr4:9497278..9497791,2	MCF-7	breast:
17	chr4:9764437..9765430-chr4:10020023..10020916,6	MCF-7	breast:
18	chr2:91818363..91818948-chr4:9766445..9767270,6	MCF-7	breast:
19	chr2:91818675..91820415-chr4:9765033..9768552,3	K562	blood:
20	chr2:91815162..91820044-chr4:9763391..9768700,25	MCF-7	breast:
21	chr4:9766486..9767204-chr4:10064960..10065893,2	MCF-7	breast:
22	chr4:9766550..9767471-chr4:10020110..10020837,2	MCF-7	breast:
23	chr1:149221736..149225365-chr4:9763717..9766826,4	MCF-7	breast:
24	chr4:9705013..9706114-chr4:10020117..10020881,3	MCF-7	breast:
25	chr4:9766848..9767385-chr4:9900038..9900893,4	MCF-7	breast:
26	chr1:149220703..149225113-chr4:9764948..9767069,4	MCF-7	breast:
27	chr4:9766226..9767390-chr4:9899951..9901032,8	MCF-7	breast:
28	chr4:9764866..9765415-chr4:9928949..9929492,2	MCF-7	breast:
29	chr2:91815178..91817122-chr4:9765055..9766792,2	K562	blood:
30	chr2:91816303..91817383-chr4:9764391..9765414,6	MCF-7	breast:
31	chr4:9704873..9705750-chr4:10016280..10017221,3	K562	blood:
32	chr2:91816400..91817015-chr4:9766701..9767270,2	MCF-7	breast:
33	chr2:91818108..91819097-chr4:9766527..9767180,2	K562	blood:
34	chr4:9705037..9705657-chr4:9778184..9778690,2	K562	blood:
35	chr4:9764428..9765300-chr4:10016550..10017565,3	K562	blood:
36	chr4:9533415..9534346-chr4:9660887..9661684,2	MCF-7	breast:
37	chr4:9761130..9763005-chr4:9988480..9990175,2	K562	blood:
38	chr4:9764792..9765537-chr4:9899989..9900954,5	MCF-7	breast:
39	chr4:9533415..9534346-chr4:9660887..9661684,2	MCF-7	breast:
40	chr4:9764370..9765339-chr4:10015197..10016013,4	MCF-7	breast:

(count:11 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DEFB131-1	chr4:9470746-9471694	NONHSAT095133
2	lnc-DRD5-16	chr4:9678932-9679558	NONHSAT095141
3	lnc-SLC2A9-1	chr4:9686325-9686330	XLOC_003881
4	lnc-SLC2A9-6	chr4:9680180-9680546	l_2603_chr4:9680179-9682164_kidney
5	lnc-DRD5-15	chr4:9680112-9680551	l_2602_chr4:9680111-9682135_thyroid
6	lnc-RP11-1396O13.13.1-3	chr4:9555234-9555605	NONHSAT095137
7	lnc-SLC2A9-1	chr4:9691882-9692319	XLOC_003881
8	lnc-SLC2A9-6	chr4:9681968-9682164	l_2603_chr4:9680179-9682164_kidney
9	lnc-SLC2A9-2	chr4:9693361-9693365	XLOC_003880
10	lnc-DRD5-15	chr4:9681973-9682135	l_2602_chr4:9680111-9682135_thyroid
11	lnc-SLC2A9-2	chr4:9682416-9682671	XLOC_003880

miRNA name	Chromosome Location	mirBase accession
hsa-miR-548i	chr4:9557878-9557899	MIMAT0005935_1

No data

Variant related genes	Relation type
OR7E85P	TF binding region
ENSG00000266246	TF binding region
ENSG00000249799	TF binding region
DRD5	TF binding region
ENPP7P11	TF binding region
OR7E84P	TF binding region
OR7E86P	TF binding region
MIR548I2	TF binding region
FAM86MP	TF binding region
DEFB131	TF binding region
ENSG00000249443	TF binding region
UNC93B7	TF binding region
ENSG00000249563	TF binding region
OR7E83P	TF binding region
ALG1L3P	TF binding region
ENSG00000265901	TF binding region
ENSG00000242034	TF binding region
OR7E35P	TF binding region
ENSG00000244004	TF binding region
OR7E85P	CpG island
ENSG00000266246	CpG island
ENSG00000249799	CpG island
DRD5	CpG island
ENPP7P11	CpG island
OR7E84P	CpG island
OR7E86P	CpG island
MIR548I2	CpG island
FAM86MP	CpG island
DEFB131	CpG island
ENSG00000249443	CpG island
UNC93B7	CpG island
ENSG00000249563	CpG island
OR7E83P	CpG island
ALG1L3P	CpG island
ENSG00000265901	CpG island
ENSG00000242034	CpG island
OR7E35P	CpG island
ENSG00000244004	CpG island
ENSG00000109667	chromatin interactions
ENSG00000206737	chromatin interactions
ENSG00000250413	chromatin interactions
FBXW7	miRNA target sites

Extended variants
information (count: 20769 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:20769 , 50 per page) page: 1 2 3 4 5 6 7 ... 416

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs568980779	chr4:9429315-9429316	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs28595731	chr4:9429332-9429333	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs28665395	chr4:9429335-9429336	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs572769345	chr4:9429343-9429344	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs540160416	chr4:9429379-9429380	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs28633849	chr4:9429395-9429396	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs574478444	chr4:9429400-9429401	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs377395883	chr4:9429413-9429414	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs542247128	chr4:9429417-9429418	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs563624890	chr4:9429436-9429437	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs531035552	chr4:9429438-9429439	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs369387108	chr4:9429440-9429441	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs546037639	chr4:9429461-9429462	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs138054196	chr4:9429472-9429473	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs6414722	chr4:9429499-9429500	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs185042569	chr4:9429539-9429540	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs547291677	chr4:9429544-9429545	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs28539709	chr4:9429545-9429546	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs528880702	chr4:9429552-9429553	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs550554503	chr4:9429554-9429555	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs568818768	chr4:9429564-9429565	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs28412316	chr4:9429598-9429599	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs551135655	chr4:9429601-9429602	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs566311230	chr4:9429603-9429604	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs142518443	chr4:9429619-9429620	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs371274201	chr4:9429624-9429625	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs188764843	chr4:9429657-9429658	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs573923335	chr4:9429676-9429677	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs535433067	chr4:9429682-9429683	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs28458944	chr4:9429687-9429688	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs376456338	chr4:9429689-9429690	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs546299968	chr4:9429698-9429699	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs28715537	chr4:9429710-9429711	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs573458546	chr4:9429712-9429713	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs540877491	chr4:9429734-9429735	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs562323354	chr4:9429761-9429762	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs529600805	chr4:9429784-9429785	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs543131191	chr4:9429785-9429786	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs147460069	chr4:9438200-9438201	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs186885167	chr4:9438236-9438237	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs572830825	chr4:9438270-9438271	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs7376091	chr4:9438283-9438284	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs114907046	chr4:9438284-9438285	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs139250000	chr4:9438302-9438303	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs191782785	chr4:9438322-9438323	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs80309866	chr4:9438323-9438324	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs149652757	chr4:9438338-9438339	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs74341411	chr4:9438348-9438349	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs537845190	chr4:9438349-9438350	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs181998881	chr4:9438354-9438355	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:63)

Disease	PMID	Source
Melanoma	20688739	CNVD
Wilms tumour	21544195	CNVD
Colorectal cancer	16272173	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17603634	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Cancer	21637783	CNVD
Melanoma	21693616	CNVD
Squamous cell cancer	21044232	CNVD
Colorectal cancer	20709793	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Non-small cell lung cancer	21044232	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Cervical cancer	21062161	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Neuroblastoma	18923191	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Breast cancer	21509527	CNVD
Lung cancer	18438408	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Schizophrenia	22241247	CNVD
Autosomal-dominant microtia	18179897	CNVD
Glioma	17123091	CNVD
Colorectal cancer	20459617	CNVD
Breast cancer	17133270	CNVD
Sezary syndrome	18413736	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Schizophrenia	23813976	CNVD
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	CNVD
Urothelial carcinoma	21177765	CNVD
Neuroblastoma	20406844	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Sinonasal adenocarcinoma	21360264	CNVD
Ependymoma	20639864	CNVD

Chromatin state (count:1569 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:9429000-9429400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr4:9429400-9429800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr4:9438200-9438600	Enhancers	Primary B cells from cord blood	blood
4	chr4:9438200-9438600	Enhancers	Primary hematopoietic stem cells	blood
5	chr4:9452600-9453800	Enhancers	Small Intestine	intestine
6	chr4:9453000-9453800	Enhancers	Duodenum Mucosa	Duodenum
7	chr4:9453600-9454800	Enhancers	Rectal Mucosa Donor 31	rectum
8	chr4:9453600-9456200	Enhancers	Fetal Intestine Large	intestine
9	chr4:9453600-9456800	Enhancers	Fetal Intestine Small	intestine
10	chr4:9453600-9457200	Enhancers	Stomach Mucosa	stomach
11	chr4:9453800-9454600	Weak transcription	Duodenum Mucosa	Duodenum
12	chr4:9454600-9454800	Enhancers	Duodenum Mucosa	Duodenum
13	chr4:9454800-9455200	Weak transcription	Duodenum Mucosa	Duodenum
14	chr4:9454800-9455800	Weak transcription	Rectal Mucosa Donor 31	rectum
15	chr4:9455200-9457200	Enhancers	Duodenum Mucosa	Duodenum
16	chr4:9455800-9456800	Enhancers	ES-I3 Cell Line	embryonic stem cell
17	chr4:9455800-9457200	Enhancers	Rectal Mucosa Donor 31	rectum
18	chr4:9456400-9456800	Enhancers	HUES6 Cell Line	embryonic stem cell
19	chr4:9456400-9457200	Enhancers	Gastric	stomach
20	chr4:9476200-9477000	Bivalent Enhancer	Fetal Brain Male	brain
21	chr4:9476600-9477000	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
22	chr4:9476600-9477000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
23	chr4:9476600-9477000	Bivalent Enhancer	Fetal Muscle Leg	muscle
24	chr4:9477000-9477400	Enhancers	Brain Inferior Temporal Lobe	brain
25	chr4:9481600-9482000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr4:9481600-9482000	Enhancers	Rectal Mucosa Donor 31	rectum
27	chr4:9481800-9482000	Enhancers	Duodenum Mucosa	Duodenum
28	chr4:9484800-9503800	Weak transcription	Right Atrium	heart
29	chr4:9495800-9496800	Enhancers	Fetal Thymus	thymus
30	chr4:9496200-9496800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr4:9496200-9496800	Enhancers	Thymus	Thymus
32	chr4:9496200-9497000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr4:9496400-9496600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr4:9496400-9496800	Enhancers	Primary hematopoietic stem cells	blood
35	chr4:9496600-9499000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr4:9496800-9499600	Weak transcription	Primary hematopoietic stem cells	blood
37	chr4:9499000-9499200	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
38	chr4:9499000-9499200	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
39	chr4:9499000-9499600	Enhancers	Liver	Liver
40	chr4:9499000-9500400	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
41	chr4:9499000-9500600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr4:9499200-9499400	Bivalent Enhancer	Fetal Thymus	thymus
43	chr4:9499200-9499600	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr4:9499200-9499800	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
45	chr4:9499200-9499800	Bivalent/Poised TSS	Brain Inferior Temporal Lobe	brain
46	chr4:9499200-9500200	Bivalent Enhancer	Primary hematopoietic stem cells short term culture	blood
47	chr4:9499200-9500200	Bivalent Enhancer	Adipose Nuclei	Adipose
48	chr4:9499200-9500400	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
49	chr4:9499200-9500400	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
50	chr4:9499200-9500600	Active TSS	H9 Cell Line	embryonic stem cell

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