Variant report

Variant	nsv834461
Chromosome Location	chr2:173979734-174038471
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:654)
CpG islands
(count:489)
Chromatin interactive
region (count:44)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:654 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr2:173982435-173982744	K562	blood:	n/a	n/a
2	ATF2	chr2:173984310-173985148	GM12878	blood:	n/a	n/a
3	ATF3	chr2:174024436-174024967	A549	lung:	n/a	n/a
4	BACH1	chr2:174010247-174010420	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr2:174035656-174035692	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr2:174010178-174010437	GM12878	blood:	n/a	n/a
7	BATF	chr2:173984302-173984545	GM12878	blood:	n/a	n/a
8	BATF	chr2:174016438-174016706	GM12878	blood:	n/a	chr2:174016621-174016632
9	BATF	chr2:174016480-174016776	GM12878	blood:	n/a	chr2:174016621-174016632
10	BCL3	chr2:174024388-174025145	A549	lung:	n/a	n/a
11	BHLHE40	chr2:173984056-173984064	K562	blood:	n/a	n/a
12	BRCA1	chr2:174016453-174017082	Hela-S3	cervix:	n/a	n/a
13	CBX3	chr2:174006412-174006821	HCT-116	colon:	n/a	n/a
14	CBX3	chr2:174024393-174024941	HCT-116	colon:	n/a	n/a
15	CBX3	chr2:174016241-174016932	HCT-116	colon:	n/a	n/a
16	CBX3	chr2:174006349-174006798	K562	blood:	n/a	n/a
17	CBX3	chr2:174006416-174006780	K562	blood:	n/a	n/a
18	CEBPB	chr2:173985710-173986091	A549	lung:	n/a	n/a
19	CEBPB	chr2:174024494-174024878	ECC-1	luminal epithelium:	n/a	chr2:174024692-174024703
20	CEBPB	chr2:174016230-174017216	HCT-116	colon:	n/a	chr2:174016682-174016695 chr2:174016955-174016972 chr2:174016958-174016971
21	CEBPB	chr2:173997458-173997559	IMR90	lung:	n/a	n/a
22	CEBPB	chr2:174014270-174014364	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr2:174024531-174024851	K562	blood:	n/a	chr2:174024692-174024703
24	CEBPB	chr2:174036685-174037276	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr2:174024619-174024766	HepG2	liver:	n/a	chr2:174024692-174024703
26	CEBPB	chr2:174030671-174030921	IMR90	lung:	n/a	chr2:174030794-174030805
27	CEBPB	chr2:174024339-174025085	HCT-116	colon:	n/a	chr2:174024692-174024703
28	CEBPB	chr2:174016278-174017167	HCT-116	colon:	n/a	chr2:174016682-174016695 chr2:174016955-174016972 chr2:174016958-174016971
29	CEBPB	chr2:174016289-174017299	A549	lung:	n/a	chr2:174016682-174016695 chr2:174016955-174016972 chr2:174016958-174016971
30	CEBPB	chr2:173985751-173986028	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr2:174030641-174030922	A549	lung:	n/a	chr2:174030794-174030805
32	CEBPB	chr2:174024427-174024829	MCF-7	breast:	n/a	chr2:174024692-174024703
33	CEBPB	chr2:174024566-174024859	K562	blood:	n/a	chr2:174024692-174024703
34	CEBPB	chr2:174024506-174024892	HepG2	liver:	n/a	chr2:174024692-174024703
35	CEBPB	chr2:174030748-174030945	K562	blood:	n/a	chr2:174030794-174030805
36	CEBPB	chr2:173999496-173999761	H1-hESC	embryonic stem cell:	n/a	n/a
37	CEBPB	chr2:174030594-174030969	Hela-S3	cervix:	n/a	chr2:174030794-174030805
38	CEBPB	chr2:173985603-173986191	IMR90	lung:	n/a	n/a
39	CEBPB	chr2:174029971-174030263	IMR90	lung:	n/a	chr2:174030203-174030215
40	CEBPB	chr2:174032043-174032123	A549	lung:	n/a	n/a
41	CEBPB	chr2:174031593-174032249	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr2:174016396-174017605	Hela-S3	cervix:	n/a	chr2:174016682-174016695 chr2:174016955-174016972 chr2:174016958-174016971
43	CEBPB	chr2:174036737-174036913	HepG2	liver:	n/a	n/a
44	CEBPB	chr2:174024466-174025117	IMR90	lung:	n/a	chr2:174024692-174024703
45	CEBPB	chr2:174016471-174017122	A549	lung:	n/a	chr2:174016682-174016695 chr2:174016955-174016972 chr2:174016958-174016971
46	CEBPB	chr2:174024368-174025010	MCF-7	breast:	n/a	chr2:174024692-174024703
47	CEBPB	chr2:174036752-174037177	A549	lung:	n/a	n/a
48	CEBPB	chr2:174030599-174031006	A549	lung:	n/a	chr2:174030794-174030805
49	CEBPB	chr2:174016364-174017130	IMR90	lung:	n/a	chr2:174016682-174016695 chr2:174016955-174016972 chr2:174016958-174016971
50	CEBPB	chr2:174024527-174024869	H1-hESC	embryonic stem cell:	n/a	chr2:174024692-174024703

(count:489 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:173983943-173983993	MCF10A-Er-Src	breast:	n/a
2	chr2:173983943-173983993	MCF10A-Er-Src	breast:	n/a
3	chr2:174030948-174030998	PANC-1	pancreas:	n/a
4	chr2:174015653-174015703	PrEC	prostate:	n/a
5	chr2:174030948-174030998	SK-N-SH	brain:	n/a
6	chr2:173989197-173989247	HL-60	blood:	n/a
7	chr2:173995795-173995845	A549	lung:	n/a
8	chr2:174030948-174030998	ovcar-3	ovarian:	n/a
9	chr2:174014462-174014512	HEEpiC	esophagus:	n/a
10	chr2:173995795-173995845	NH-A	brain:	n/a
11	chr2:174014462-174014512	HepG2	liver:	n/a
12	chr2:173989197-173989247	PFSK-1	brain:	n/a
13	chr2:173989197-173989247	HRCEpiC	kidney:	n/a
14	chr2:174024669-174024719	NT2-D1	testis:	n/a
15	chr2:173983943-173983993	Jurkat	blood:	n/a
16	chr2:173983943-173983993	A549	lung:	n/a
17	chr2:173983943-173983993	SK-N-SH	brain:	n/a
18	chr2:174014462-174014512	SAEC	small airway:	n/a
19	chr2:173995795-173995845	Hepatocyte	liver:	n/a
20	chr2:173989197-173989247	LNCaP	prostate:	n/a
21	chr2:173999776-173999826	Hela-S3	cervix:	n/a
22	chr2:174024669-174024719	NHBE	bronchial:	n/a
23	chr2:173995795-173995845	SK-N-SH_RA	brain:	n/a
24	chr2:173995795-173995845	HRCEpiC	kidney:	n/a
25	chr2:173995795-173995845	HAEpiC	amniotic membrane:	n/a
26	chr2:174015653-174015703	SK-N-SH	brain:	n/a
27	chr2:174030948-174030998	GM19239	blood:	n/a
28	chr2:174030948-174030998	MCF-7	breast:	n/a
29	chr2:173989197-173989247	PrEC	prostate:	n/a
30	chr2:173995795-173995845	K562	blood:	n/a
31	chr2:174015653-174015703	GM12891	blood:	n/a
32	chr2:173999776-173999826	AG10803	skin:	n/a
33	chr2:174015653-174015703	SK-N-MC	brain:	n/a
34	chr2:174024669-174024719	SAEC	small airway:	n/a
35	chr2:174015653-174015703	Hela-S3	cervix:	n/a
36	chr2:174015653-174015703	HMEC	breast:	n/a
37	chr2:174024669-174024719	HNPCEpiC	eye:	n/a
38	chr2:173999776-173999826	HIPEpiC	eye:	n/a
39	chr2:173999776-173999826	NH-A	brain:	n/a
40	chr2:173999776-173999826	HL-60	blood:	n/a
41	chr2:173995795-173995845	AG10803	skin:	n/a
42	chr2:174030948-174030998	Caco-2	colon:	n/a
43	chr2:173999776-173999826	PrEC	prostate:	n/a
44	chr2:174015653-174015703	SKMC	muscle:	n/a
45	chr2:174030948-174030998	BE2_C	brain:	n/a
46	chr2:174014462-174014512	HRPEpiC	eye:	n/a
47	chr2:174024669-174024719	GM12878	blood:	n/a
48	chr2:173983943-173983993	AG04450	lung:	fetal
49	chr2:173995795-173995845	AG04449	skin:	fetal
50	chr2:173999776-173999826	HRCEpiC	kidney:	n/a

(count:44 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:174011042..174014620-chr2:174016771..174020819,3	MCF-7	breast:
2	chr2:174023781..174025483-chr2:174027611..174029540,2	K562	blood:
3	chr2:173985743..173988657-chr2:173992178..173994964,4	K562	blood:
4	chr2:173997780..173999640-chr2:174139460..174141326,2	K562	blood:
5	chr2:173987726..173990212-chr8:91575317..91577532,2	MCF-7	breast:
6	chr2:174002531..174005175-chr2:174006407..174008888,2	K562	blood:
7	chr2:173984313..173986145-chr2:174000208..174002832,2	K562	blood:
8	chr2:174027701..174029324-chr2:174034830..174037383,2	K562	blood:
9	chr2:173998706..174001151-chr2:174010395..174012464,2	K562	blood:
10	chr2:173972338..173974560-chr2:173994516..173997449,2	K562	blood:
11	chr2:174024599..174026346-chr2:174036575..174038101,2	K562	blood:
12	chr2:173996961..173999501-chr2:174001497..174003387,2	K562	blood:
13	chr2:173902260..173904041-chr2:173982798..173984543,2	MCF-7	breast:
14	chr2:173988691..173991779-chr2:173993829..173996976,3	K562	blood:
15	chr2:173945072..173946599-chr2:174032993..174034733,2	K562	blood:
16	chr2:173944994..173946697-chr2:174012717..174014873,2	MCF-7	breast:
17	chr2:173938732..173942486-chr2:173997338..174001096,5	K562	blood:
18	chr2:173988691..173991779-chr2:173993829..173996976,3	K562	blood:
19	chr2:174016557..174018209-chr2:174020513..174022324,2	MCF-7	breast:
20	chr2:173912619..173914756-chr2:174014173..174017350,3	MCF-7	breast:
21	chr2:173942302..173944887-chr2:173980344..173983035,2	K562	blood:
22	chr2:174001713..174004612-chr2:174011601..174013779,2	K562	blood:
23	chr2:173892227..173892797-chr2:174021959..174022854,2	MCF-7	breast:
24	chr2:174031458..174032993-chr2:174038547..174040630,2	K562	blood:
25	chr2:173989210..173991573-chr2:173993201..173996190,3	MCF-7	breast:
26	chr2:173989210..173991573-chr2:173993201..173996190,3	MCF-7	breast:
27	chr2:173994976..173996675-chr2:173999550..174001864,2	MCF-7	breast:
28	chr2:173969673..173972260-chr2:173985916..173987500,2	MCF-7	breast:
29	chr2:174011042..174014620-chr2:174016771..174020819,3	MCF-7	breast:
30	chr2:173938869..173942300-chr2:173999393..174002549,3	K562	blood:
31	chr2:173938392..173941767-chr2:173987528..173992085,5	MCF-7	breast:
32	chr2:174001713..174004612-chr2:174011601..174013779,2	K562	blood:
33	chr2:174034052..174036635-chr2:174040991..174043810,2	MCF-7	breast:
34	chr2:173985743..173988657-chr2:173992178..173994964,4	K562	blood:
35	chr2:173959860..173961985-chr2:173986864..173989225,2	MCF-7	breast:
36	chr2:173972593..173975547-chr2:173981865..173984989,3	MCF-7	breast:
37	chr2:174016557..174018209-chr2:174020513..174022324,2	MCF-7	breast:
38	chr2:174027701..174029324-chr2:174034830..174037383,2	K562	blood:
39	chr2:174002531..174005175-chr2:174006407..174008888,2	K562	blood:
40	chr2:173998706..174001151-chr2:174010395..174012464,2	K562	blood:
41	chr2:173951489..173953627-chr2:173981191..173983390,3	K562	blood:
42	chr2:173994976..173996675-chr2:173999550..174001864,2	MCF-7	breast:
43	chr2:173996961..173999501-chr2:174001497..174003387,2	K562	blood:
44	chr2:173984313..173986145-chr2:174000208..174002832,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SP3-3	chr2:174031174-174031566	ENSG00000238133.2
2	lnc-SP3-3	chr2:174031458-174031566	ENSG00000238133.2

No data

Variant related genes	Relation type
ENSG00000091436	TF binding region
ENSG00000091436	CpG island
ENSG00000091428	chromatin interactions
ENSG00000091436	chromatin interactions

Extended variants
information (count: 2070 )
Associated
traits (count: 46 )

Variant overlapped rSNPs/rCNVs (count:2070 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs188319122	chr2:173979769-173979770	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs536361127	chr2:173979770-173979771	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs201241353	chr2:173979799-173979800	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs529271657	chr2:173979800-173979801	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs181084264	chr2:173979804-173979805	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs376680681	chr2:173979806-173979807	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs566416780	chr2:173979966-173979967	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs545044781	chr2:173980016-173980017	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs369372507	chr2:173980048-173980049	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs527611260	chr2:173980117-173980118	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs552085377	chr2:173980119-173980120	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs570669217	chr2:173980120-173980121	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs537501737	chr2:173980121-173980122	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs565123148	chr2:173980144-173980145	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs185780004	chr2:173980211-173980212	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs535456368	chr2:173980254-173980255	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs553837914	chr2:173980429-173980430	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs572754491	chr2:173980445-173980446	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs546520806	chr2:173980451-173980452	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs558058900	chr2:173980463-173980464	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs576583274	chr2:173980472-173980473	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs543525213	chr2:173980495-173980496	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs113292669	chr2:173980541-173980542	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs561862822	chr2:173980554-173980555	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs529382111	chr2:173980562-173980563	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs541007953	chr2:173980572-173980573	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs150304719	chr2:173980580-173980581	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs78559861	chr2:173980588-173980589	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs377275568	chr2:173980595-173980596	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs552456892	chr2:173980650-173980651	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs370956045	chr2:173980670-173980671	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs541142453	chr2:173980681-173980682	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs376358239	chr2:173980690-173980691	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs531554759	chr2:173980708-173980709	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs78457433	chr2:173980719-173980720	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs114309736	chr2:173980731-173980732	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs202173798	chr2:173980742-173980743	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs80052012	chr2:173980759-173980760	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs553799060	chr2:173980764-173980765	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs546538399	chr2:173980768-173980769	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs371331480	chr2:173980770-173980771	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs565718485	chr2:173980817-173980818	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs539698845	chr2:173980819-173980820	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs558447833	chr2:173980867-173980868	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs190494699	chr2:173980869-173980870	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs543981717	chr2:173980894-173980895	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs183145246	chr2:173980906-173980907	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs573795820	chr2:173980965-173980966	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs541169542	chr2:173980967-173980968	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs547357143	chr2:173980991-173980992	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:46)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Ependymoma	16718352	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	18522746	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	16272173	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Autism	16446308	CNVD
Autism	19401682	CNVD
Colorectal cancer	16272173	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
Glioblastoma	21080181	CNVD
small cell lung cancer	20016488	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Prostate cancer	16573809	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Donnai-Barrow syndrome	21085971	CNVD
Breast cancer	21045282	CNVD
Limb abnormalities	22140379	CNVD
Sudden cardiac death	19188705	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Breast cancer	21364760	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1313 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:173945400-173991200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr2:173953800-173991400	Weak transcription	Primary hematopoietic stem cells	blood
3	chr2:173955600-173984000	Weak transcription	Gastric	stomach
4	chr2:173957800-173983800	Weak transcription	Fetal Muscle Leg	muscle
5	chr2:173958000-173983800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr2:173962200-173983800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr2:173965000-173987400	Weak transcription	Primary monocytes fromperipheralblood	blood
8	chr2:173965400-173984400	Weak transcription	Aorta	Aorta
9	chr2:173965400-173987200	Weak transcription	Dnd41	blood
10	chr2:173965400-173989200	Weak transcription	Duodenum Smooth Muscle	Duodenum
11	chr2:173965600-173983800	Weak transcription	Adipose Nuclei	Adipose
12	chr2:173968600-173990600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
13	chr2:173969200-173987600	Weak transcription	Monocytes-CD14+_RO01746	blood
14	chr2:173970000-173983200	Weak transcription	Right Atrium	heart
15	chr2:173971600-173985600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
16	chr2:173971800-173980400	Weak transcription	Ovary	ovary
17	chr2:173972200-173980200	Weak transcription	Psoas Muscle	Psoas
18	chr2:173972200-173983800	Weak transcription	Lung	lung
19	chr2:173972600-173983800	Weak transcription	Right Ventricle	heart
20	chr2:173973200-173983800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr2:173974400-173980400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
22	chr2:173974400-174005200	Weak transcription	Fetal Intestine Small	intestine
23	chr2:173974600-173983800	Weak transcription	Stomach Smooth Muscle	stomach
24	chr2:173974600-173984000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
25	chr2:173974600-173984400	Weak transcription	NHEK	skin
26	chr2:173974800-173982600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
27	chr2:173974800-173982600	Weak transcription	A549	lung
28	chr2:173974800-173983000	Weak transcription	Fetal Heart	heart
29	chr2:173974800-173983000	Weak transcription	Osteobl	bone
30	chr2:173974800-173983200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr2:173974800-173983200	Weak transcription	NHDF-Ad	bronchial
32	chr2:173974800-173983800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr2:173974800-173984000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr2:173974800-173988600	Weak transcription	HSMM	muscle
35	chr2:173974800-173991400	Weak transcription	K562	blood
36	chr2:173977400-173980400	Weak transcription	Skeletal Muscle Female	skeletal muscle
37	chr2:173978200-173995200	Weak transcription	Cortex derived primary cultured neurospheres	brain
38	chr2:173979400-173980200	Weak transcription	GM12878-XiMat	blood
39	chr2:173979600-173981200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr2:173980000-173985800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
41	chr2:173980200-173980600	Enhancers	Psoas Muscle	Psoas
42	chr2:173980400-173980600	Enhancers	Esophagus	oesophagus
43	chr2:173980400-173980600	Enhancers	Skeletal Muscle Female	skeletal muscle
44	chr2:173980400-173981400	Enhancers	Breast Myoepithelial Primary Cells	Breast
45	chr2:173980400-173981400	Enhancers	Ovary	ovary
46	chr2:173980400-173982400	Enhancers	Left Ventricle	heart
47	chr2:173980600-173981200	Weak transcription	Skeletal Muscle Female	skeletal muscle
48	chr2:173980600-173983200	Weak transcription	Psoas Muscle	Psoas
49	chr2:173980600-173989200	Weak transcription	Esophagus	oesophagus
50	chr2:173981000-173981400	Enhancers	Skeletal Muscle Male	skeletal muscle

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